ENST00000205402.10:c.1157A>G
MANE Select
|
ENSP00000205402.3:p.Tyr386Cys
|
|
ENST00000205402.9:c.1157A>G
|
ENSP00000205402.3:p.Tyr386Cys
|
|
ENST00000415325.5:c.*831A>G
|
ENSP00000402593.1:n.*831A>G
|
|
ENST00000417551.5:c.1157A>G
|
ENSP00000390667.1:p.Tyr386Cys
|
|
ENST00000437604.6:c.1013A>G
|
ENSP00000387542.2:p.Tyr338Cys
|
|
ENST00000440410.5:c.1088A>G
|
ENSP00000417016.1:p.Tyr363Cys
|
|
NM_000108.4:c.1157A>G
|
NP_000099.2:p.Tyr386Cys
|
|
NM_001289750.1:c.860A>G
|
NP_001276679.1:p.Tyr287Cys
|
|
NM_001289751.1:c.1088A>G
|
NP_001276680.1:p.Tyr363Cys
|
|
NM_001289752.1:c.1013A>G
|
NP_001276681.1:p.Tyr338Cys
|
|
NM_000108.5:c.1157A>G
MANE Select
|
NP_000099.2:p.Tyr386Cys
|
|